Author:
Bougacha-Elleuch Noura,Charfi Nadia,Miled Nabil,Bouhajja Houda,Belguith Neila,Mnif Mouna,Jaurge Paula,Chikhrouhou Nessrine,Ayadi Hammadi,Hachicha Mongia,Abid Mohamed
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference49 articles.
1. Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR (2010) A method and server for predicting damaging missense mutations. Nat Methods 7(4):248–249
2. Ambrugger P, Stoeva I, Biebermann H, Torresani T, Leitner C, Grüters A (2001) Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism. Eur J Endocrinol 145(1):19–24
3. Avbelj M, Tahirovic H, Debeljak M, Kusekova M, Toromanovic A, Krzisnik C, Battelino T (2007) High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis. Eur J Endocrinol 156(5):511–519
4. Bahn RS, Castro MRJ (2011) Approach to the patient with nontoxic multinodular goiter. J Clin Endocrinol Metab 96(5):1202–1212
5. Baş VN, Aycan Z, Cangul H, Kendall M, Ağladıoğlu SY, Çetinkaya S, Maher ER (2014) A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect. J Pediatr Endocrinol Metab 27(3–4):383–387
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献